Atrial septal defect 3

Preferred Label : Atrial septal defect 3;

Symbol : ASD3;

CISMeF acronym : ASD3;

Type : Phenotype, molecular basis known;

Prefixed ID : #614089;

Details

Origin ID

614089;

UMLS CUI

C3279790;

Automatic exact mappings (from CISMeF team)
- Atrial septal defect, ostium secundum type [ORDO Disease]
Currated CISMeF NLP mapping
- atrial heart septal defect 3 [DO Concept]
- atrial septal defect 3 [MeSH concept]
- atrial septal defect 3 [MeSH Supplementary Concept]
DO Cross reference
- atrial heart septal defect 3 [DO Concept]
Genes related to phenotype
- Myosin, heavy chain 6, cardiac muscle, alpha [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Secundum atrial septal defect [HPO term]
ORDO concept(s)
- Atrial septal defect, ostium secundum type [ORDO Disease]
- Interatrial communication [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrial septal defect 3 [MeSH concept]
- atrial septal defect 3 [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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